AR035431A1 - 6,7,8,9-tetrahidro-5h-benzocicloheptenil aminas aciladas, un metodo para su sintesis, composiciones farmaceuticas y el uso de dichos compuestos para la fabricacion de medicamentos - Google Patents
6,7,8,9-tetrahidro-5h-benzocicloheptenil aminas aciladas, un metodo para su sintesis, composiciones farmaceuticas y el uso de dichos compuestos para la fabricacion de medicamentosInfo
- Publication number
- AR035431A1 AR035431A1 ARP020100441A ARP020100441A AR035431A1 AR 035431 A1 AR035431 A1 AR 035431A1 AR P020100441 A ARP020100441 A AR P020100441A AR P020100441 A ARP020100441 A AR P020100441A AR 035431 A1 AR035431 A1 AR 035431A1
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- Prior art keywords
- alkyl
- group
- phenyl
- substituents
- independently
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Links
- 150000001412 amines Chemical class 0.000 title abstract 2
- 230000015572 biosynthetic process Effects 0.000 title abstract 2
- 150000001875 compounds Chemical class 0.000 title abstract 2
- 239000003814 drug Substances 0.000 title abstract 2
- 238000004519 manufacturing process Methods 0.000 title abstract 2
- 238000000034 method Methods 0.000 title abstract 2
- 239000008194 pharmaceutical composition Substances 0.000 title abstract 2
- 238000003786 synthesis reaction Methods 0.000 title abstract 2
- 125000001424 substituent group Chemical group 0.000 abstract 25
- 229910052736 halogen Inorganic materials 0.000 abstract 15
- 150000002367 halogens Chemical class 0.000 abstract 15
- 125000001072 heteroaryl group Chemical group 0.000 abstract 15
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 15
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 13
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 abstract 12
- 125000002577 pseudohalo group Chemical group 0.000 abstract 12
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 11
- 125000006274 (C1-C3)alkoxy group Chemical group 0.000 abstract 9
- -1 alkoxy mercapto Chemical class 0.000 abstract 6
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 5
- 125000003118 aryl group Chemical group 0.000 abstract 5
- 125000003545 alkoxy group Chemical group 0.000 abstract 4
- 125000000217 alkyl group Chemical group 0.000 abstract 4
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 3
- 125000005842 heteroatom Chemical group 0.000 abstract 3
- 125000000623 heterocyclic group Chemical group 0.000 abstract 3
- 229910052757 nitrogen Inorganic materials 0.000 abstract 3
- 229910052760 oxygen Inorganic materials 0.000 abstract 3
- 229910052717 sulfur Inorganic materials 0.000 abstract 3
- 125000000027 (C1-C10) alkoxy group Chemical group 0.000 abstract 2
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 2
- 125000001637 1-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C(*)=C([H])C([H])=C([H])C2=C1[H] 0.000 abstract 2
- 125000001622 2-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C(*)C([H])=C([H])C2=C1[H] 0.000 abstract 2
- 125000006374 C2-C10 alkenyl group Chemical group 0.000 abstract 2
- 125000000304 alkynyl group Chemical group 0.000 abstract 2
- 125000004103 aminoalkyl group Chemical group 0.000 abstract 2
- 125000004104 aryloxy group Chemical group 0.000 abstract 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 2
- 125000002618 bicyclic heterocycle group Chemical group 0.000 abstract 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 2
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 1
- KKJUPNGICOCCDW-UHFFFAOYSA-N 7-N,N-Dimethylamino-1,2,3,4,5-pentathiocyclooctane Chemical compound CN(C)C1CSSSSSC1 KKJUPNGICOCCDW-UHFFFAOYSA-N 0.000 abstract 1
- 208000004476 Acute Coronary Syndrome Diseases 0.000 abstract 1
- 206010002383 Angina Pectoris Diseases 0.000 abstract 1
- 206010003210 Arteriosclerosis Diseases 0.000 abstract 1
- 208000024172 Cardiovascular disease Diseases 0.000 abstract 1
- 208000002249 Diabetes Complications Diseases 0.000 abstract 1
- 206010048554 Endothelial dysfunction Diseases 0.000 abstract 1
- 208000010228 Erectile Dysfunction Diseases 0.000 abstract 1
- 208000007530 Essential hypertension Diseases 0.000 abstract 1
- 206010018367 Glomerulonephritis chronic Diseases 0.000 abstract 1
- 206010019280 Heart failures Diseases 0.000 abstract 1
- 206010020772 Hypertension Diseases 0.000 abstract 1
- JCXJVPUVTGWSNB-UHFFFAOYSA-N Nitrogen dioxide Chemical group O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 abstract 1
- 208000001132 Osteoporosis Diseases 0.000 abstract 1
- 201000001068 Prinzmetal angina Diseases 0.000 abstract 1
- 201000003099 Renovascular Hypertension Diseases 0.000 abstract 1
- 208000017442 Retinal disease Diseases 0.000 abstract 1
- 206010038923 Retinopathy Diseases 0.000 abstract 1
- 201000004239 Secondary hypertension Diseases 0.000 abstract 1
- 208000007718 Stable Angina Diseases 0.000 abstract 1
- 208000006011 Stroke Diseases 0.000 abstract 1
- 208000007536 Thrombosis Diseases 0.000 abstract 1
- 208000007814 Unstable Angina Diseases 0.000 abstract 1
- 208000009325 Variant Angina Pectoris Diseases 0.000 abstract 1
- 206010047281 Ventricular arrhythmia Diseases 0.000 abstract 1
- 125000001931 aliphatic group Chemical group 0.000 abstract 1
- 125000003282 alkyl amino group Chemical group 0.000 abstract 1
- MDFFNEOEWAXZRQ-UHFFFAOYSA-N aminyl Chemical group [NH2] MDFFNEOEWAXZRQ-UHFFFAOYSA-N 0.000 abstract 1
- 230000033115 angiogenesis Effects 0.000 abstract 1
- 208000011775 arteriosclerosis disease Diseases 0.000 abstract 1
- 210000001367 artery Anatomy 0.000 abstract 1
- 208000006673 asthma Diseases 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 208000020832 chronic kidney disease Diseases 0.000 abstract 1
- 208000022831 chronic renal failure syndrome Diseases 0.000 abstract 1
- 208000019425 cirrhosis of liver Diseases 0.000 abstract 1
- 229940124558 contraceptive agent Drugs 0.000 abstract 1
- 239000003433 contraceptive agent Substances 0.000 abstract 1
- 208000029078 coronary artery disease Diseases 0.000 abstract 1
- 230000003247 decreasing effect Effects 0.000 abstract 1
- 206010012601 diabetes mellitus Diseases 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 230000002526 effect on cardiovascular system Effects 0.000 abstract 1
- 230000008694 endothelial dysfunction Effects 0.000 abstract 1
- 230000003511 endothelial effect Effects 0.000 abstract 1
- 201000001881 impotence Diseases 0.000 abstract 1
- 125000003392 indanyl group Chemical group C1(CCC2=CC=CC=C12)* 0.000 abstract 1
- 208000030603 inherited susceptibility to asthma Diseases 0.000 abstract 1
- 208000017169 kidney disease Diseases 0.000 abstract 1
- 230000006386 memory function Effects 0.000 abstract 1
- 125000005358 mercaptoalkyl group Chemical group 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 208000010125 myocardial infarction Diseases 0.000 abstract 1
- 230000002093 peripheral effect Effects 0.000 abstract 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 abstract 1
- 125000003386 piperidinyl group Chemical group 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- 208000002815 pulmonary hypertension Diseases 0.000 abstract 1
- 125000000719 pyrrolidinyl group Chemical group 0.000 abstract 1
- 208000037803 restenosis Diseases 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
Classifications
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- C07—ORGANIC CHEMISTRY
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- C07C235/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms
- C07C235/42—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings and singly-bound oxygen atoms bound to the same carbon skeleton
- C07C235/44—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings and singly-bound oxygen atoms bound to the same carbon skeleton with carbon atoms of carboxamide groups and singly-bound oxygen atoms bound to carbon atoms of the same non-condensed six-membered aromatic ring
- C07C235/54—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings and singly-bound oxygen atoms bound to the same carbon skeleton with carbon atoms of carboxamide groups and singly-bound oxygen atoms bound to carbon atoms of the same non-condensed six-membered aromatic ring having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a ring other than a six-membered aromatic ring
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- C07C233/00—Carboxylic acid amides
- C07C233/64—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings
- C07C233/65—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atoms of the carboxamide groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals
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- C07C233/67—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms
- C07C233/74—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a ring other than a six-membered aromatic ring
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- C07C2602/04—One of the condensed rings being a six-membered aromatic ring
- C07C2602/12—One of the condensed rings being a six-membered aromatic ring the other ring being at least seven-membered
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Abstract
Una 6,7,8,9-tetrahidro-5H-benzocicloheptenil-amina acilada caracterizada porque la fórmula general (1) en cualquiera de sus formas estereoisómeras o una de sus mezclas en cualquier proporción o una de sus sales farmacéuticamente aceptables, en la que: R1 y R4 se seleccionan, independientemente uno de otro, del grupo formado por: H, alquilo C1-10, alquenilo C2-10 y alquinilo C2-10 no sustituidos y al menos monosustituidos, cuyos sustituyentes se seleccionan del grupo formado por F, OH, alcoxi C1-8 mercapto, CN, COOR6, CONR7R8 y fenilo y heteroarilo no sustituidos y al menos monosustituidos, cuyos sustituyentes se seleccionan del grupo formado por halógenos, pseudohalógenos, alquilo C1-3, alcoxi C1-3 y CF3, fenilo y heteroarilo no sustituidos y al menos monosustituidos, cuyos sustituyentes se seleccionan del grupo formado por halógenos, pseudohalógenos, alquilo C1-3, alcoxi C1-3 y CF3, R9CO, CONR10R11, COOR2, CF3, halógenos, pseudohalógenos, NR13R14, OR15, S(O)mR16, SO2NR17R18 y NO2; R2 y R3 se seleccionan, independientemente uno de otro, a partir del grupo formado por: H, halógenos, pseudohalógenos, alquilo C1-10 no sustituido y al menos monosustituido, cuyos sustituyentes se seleccionan del grupo formado por OH, fenilo y heteroarilo, OH, fenilo y heteroarilo, OH, alcoxi C1-10, fenoxi, S(O)mR19, CF3, CN, NO2, alquil C1-10 amino, di-alquil C1-10 amino, alquil C1-6-CONH-, fenil-CONH- y fenil-SO2-O- no sustituidos y al menos monosustituidos, cuyos sustituyentes se seleccionan del grupo formado por halógenos, pseudohalógenos, CH3, y metoxi, alquil C1-6 SO2-O-, alquil C1-6 CO no sustituidos y al menos monosustituidos, cuyos sustituyentes se seleccionan del grupo formado por F, di-alquil C1-3 amino, pirrolidinilo y piperidinilo, y fenil-CO, cuya parte fenilo puede estar sustituida por uno o más sustituyentes del grupo formado por alquilo C1-3, halógenos y metoxi; A se selecciona del grupo formado por CH2, CHOH y CH-alquilo C1-3; B se selecciona del grupo formado por CH2 y CH-alquilo C1-3; C, independientemente, tiene el mismo significado que B; D, independientemente, tiene el mismo significado que B; R5 es un grupo Ar o un grupo Hetar, ambos de los cuales pueden estar no sustituidos o llevar uno o más sustituyentes seleccionados del grupo formado por halógenos, pseudohalógenos, NH2, alquilo C1-10, alquenilo C2-10, alquinilo C2-10, alcoxi C1-10, alquil C1-10 amino y di-alquil C1-10 amino no sustituidos y al menos monosustituidos, cuyos sustituyentes se seleccionan del grupo formado por F, OH, alcoxi C1-8, ariloxi, alquil C1-8 mercapto, NH2, alquil C1-8 amino y di-alquil C1-8 amino, alcanodiil C3-5, fenilo, heteroarilo, alquilo C1-4 sustituido con arilo o heteroarilo, CF3, NO2, OH, fenoxi, bencil-oxi, alquil C1-10 COO, S(O)mR20, SH, fenilamino, bencilamino, alquil C1-10-CONH-, alquil C1-10-CON-alquilo C1-4, fenil-CONH-, fenil-CON-alquilo C1-4, heteroaril-CONH-, heteroaril-CON-alquilo C1-4, alquil C1-10-CO, fenil-CO, heteroaril-CO, CF3-CO, -OCH2O-, OCF2O-, OCH2CH2O-, -CH2CH2O-, COOR21, CONR22R23, CNH(NCH2), SO2NR24R25, R26SO2NH-, R27SO2N-alquilo C1-6, y heterociclos de 5 a 7 miembros mononucleares, alifáticos, saturados o al menos monoinsaturados, que contienen 1 a 3 heteroátomos seleccionados del grupo formado por N, O y S, heterociclos que pueden estar sustituidos con uno o más sustituyentes seleccionados del grupo formado por halógenos, alquilo C1-3, alcoxi C1-3, OH, oxo y CF3, donde dichos heterociclos pueden estar opcionalmente condensados con dicho grupo Ar o dicho Hetar, donde todos los grupos arilo, heteroarilo, fenilo, que contiene arilo que contienen heteroarilo y que contienen fenilo, que están presentes opcionalmente en dichos sustituyentes de dicho grupo Ar o dicho grupo Hetar, pueden estar sustituidos con uno o más sustituyentes seleccionados del grupo formado por halógenos, pseudohalógenos, alquilo C1-3, OH, alcoxi C1-3 y CF3; R6 se selecciona del grupo formado por: H, alquilo C1-10 que puede estar sustituido con uno o más sustituyentes seleccionados del grupo formado por F, alcoxi C1-8 y di-alquil C1-8 amino, aril-alquilo C1-4 y heteroaril-alquilo C1-4, que pueden estar sustituidos con uno o más sustituyentes seleccionados del grupo formado por halógenos, alcoxi C1-4 y di-alquil C1-6 amino; R7 se selecciona del grupo formado por: H, alquilo C1-10 que puede estar sustituido con uno o más sustituyentes seleccionados del grupo formado por F, alcoxi C1-8, di-alquil C1-8 amino y fenilo, fenilo, indanilo y heteroarilo, y donde cada uno de los grupos aromáticos mencionado anteriormente puede estar no sustituido o llevar uno o más sustituyentes del grupo formado por halógenos, pseudohalógenos, alquilo C1-3, alcoxi C1-3 y CF3; R8 es H o alquilo C1-10; R9 se selecciona del grupo formado por: alquilo C1-10 que puede estar no sustituido o llevar uno o más sustituyentes del grupo formado por: F, alcoxi C1-4, di-alquil C1-3 amino, y fenilo y heteroarilo no sustituidos y al menos monosustituidos, cuyos sustituyentes se seleccionan del grupo formado por alquilo C1-3, alcoxi C1-3, halógenos, pseudohalógenos y CF3; R10, independientemente, tiene el mismo significado que R7; R11, independientemente, tiene el mismo significado que R8; R12, independientemente, tiene el mismo significado que R6; R13 se selecciona del grupo formado por: H, alquilo C1-6, fenilo, bencilo, heteroarilo, alquil C1-6-CO, fenil-CO y heteroaril-CO no sustituidos y sustituidos, cuyos sustituyentes se seleccionan del grupo formado por halógenos, pseudohalógenos, alquilo C1-3, alcoxi C1-3 y CF3, y donde pueden estar presentes uno o más de estos sustituyentes; R14, independientemente, tiene el mismo significado que R13; R15 se selecciona del grupo formado por: H, alquilo C1-10, alcoxi C1-3-alquilo C1-3 y bencilo, fenilo y heteroarilo sustituidos y no sustituidos, cuyos sustituyentes se seleccionan del grupo formado por halógenos, pseudohalógenos, alquilo C1-3, alcoxi C1-3 y CF3, y donde pueden estar presentes uno o más de esos sustituyentes; R16 se selecciona del grupo formado por: alquilo C1-10 que puede estar sustituidos con uno o más sustituyentes seleccionados del grupo formado por F, OH, alcoxi C1-8, ariloxi, alquil C1-8 mercapto, alquil C1-8 amino y di-alquil C1-8 amino, CF3 y fenilo y heteroarilo sustituido y no sustituido, cuyos sustituyentes se seleccionan del grupo formado por halógenos, pseudohalógenos, alquilo C1-3, alcoxi C1-3 y CF3, y donde pueden estar presentes uno o más de estos sustituyentes; R17, independientemente, tiene el mismo significado que R7; R18, independientemente, tiene el mismo significado que R8; R19 independientemente, tiene el mismo significado que R16; R20, independientemente, tiene el mismo significado que R16; R21, independientemente, tiene el mismo significado que R6; R22, independientemente, tiene el mismo significado que R7; R23, independientemente, tiene el mismo significado que R8; R24, independientemente, tiene el mismo significado que R7; R25, independientemente, tiene el mismo significado que R8; R26, independientemente, tiene el mismo significado que R16; R17, independientemente, tiene el mismo significado que R16; heteroarilo es un heterociclo mono- o bicíclico, aromático de 5 a 10 miembros, que contiene uno o más heteroátomos seleccionados del grupo formado por N, O y S; el grupo Hetar es un heterociclo mono- o bicíclico, aromático de 5 a 10 miembros, que contiene uno o más heteroátomos seleccionados del grupo formado por N, O y S; arilo es fenilo, naft-1-ilo o naft-2-ilo; el grupo Ar es fenilo, naft-1-ilo o naft-2-ilo; m es 0, 1 o 2; un método para su síntesis, composiciones farmacéuticas y el uso de dichos compuestos útiles para la fabricación de medicamentos para el tratamiento de enfermedades cardiovasculares, angina de pecho estable e inestable, cardiopatía coronaria, angina de Prinzmetal, síndrome agudo de las coronarias, insuficiencia cardíaca, infarto de miocardio, ataque de apoplejía, trombosis, enfermedad oclusiva de las arterias periféricas, disfunción endotelial, arteriosclerosis, restenosis, dano endotelial después de PTCA, hipertensión, hipertensión esencial, hipertensión pulmonar, hipertensión secundaria, hipertensión renovascular, glomerulonefritis crónica, disfunción eréctil, arritmia ventricular, diabetes, complicaciones de la diabetes, nefropatía, retinopatía, angiogénesis, asma bronquial, insuficiencia renal crónica, cirrosis hepática, osteoporosis, o funcionamiento limitado de la memoria o capacidad de aprendizaje limitada, o disminución del riesgo cardiovascular de las mujeres menopáusicas o después de ingerir contraceptivos.
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| BG (1) | BG108060A (es) |
| BR (1) | BR0207197A (es) |
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| CZ (1) | CZ20032134A3 (es) |
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| DK (1) | DK1362027T3 (es) |
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| HR (1) | HRP20030645A2 (es) |
| HU (1) | HUP0303133A3 (es) |
| IL (2) | IL157211A0 (es) |
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